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University of Utah Health Research · 9 hours ago

Clinical Research Coordinators (Non-R.N.)

Salt Lake City, UT

Full-time

Hybrid

Mid, Senior Level

$30K/yr - $83K/yr

4+ years exp

University of Utah Health Research is seeking Clinical Research Coordinators (Non-R.N.) to coordinate day-to-day clinical trial activities. The role involves ensuring compliance with Good Clinical Practice, managing study protocols, and working directly with study participants to facilitate research processes.

Higher Education

Responsibilities

Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations

Implement processes and organize efforts within study team to achieve objectives, coordinating research procedures, study visits, and follow-up care

Create and maintain tools and documentation to track study metrics, providing updates to management

Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities

Maintain source documents and report adverse events

Recruit, screen, enroll, and obtain consent from study participants

Collect and maintain patient and laboratory data

Work directly with study participants and families and serve as project liaison to other departments, outside organizations, and government agencies

Works under the direction of the Primary Investigator (PI)

Requires moderate skill set and proficiency in discipline

Conducts work assignments of increasing complexity, under moderate supervision with some latitude for independent judgment

Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations

Implement processes and organize efforts within study team to achieve objectives, coordinating research procedures, study visits, and follow-up care

Create and maintain tools and documentation to track study metrics, providing updates to management

Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities

Maintain source documents and report adverse events

Recruit, screen, enroll, and obtain consent from study participants

Collect and maintain patient and laboratory data

Work directly with study participants and families and serve as project liaison to other departments, outside organizations, and government agencies

Works under the direction of the Primary Investigator (PI)

Considered highly skilled and proficient in discipline

Conducts complex, important work under minimal supervision and with wide latitude for independent judgment

Qualification

Clinical Practice (GCP)Clinical trial coordinationIRB protocol developmentPatient data managementAdverse event reportingCommunication skillsTeam collaborationProblem-solving

Required

Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience for Clinical Research Coordinator (Non-R.N.), II

Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience for Clinical Research Coordinator (Non-R.N.), III

Coordinate day-to-day clinical trial activities in compliance with Good Clinical Practice (GCP), study protocols, and applicable IRB regulations

Implement and manage processes to support study objectives, including development and maintenance of IRB protocols, coordination of research procedures, study visits, and follow-up care

Create and maintain tracking tools and documentation to monitor study metrics and provide regular updates to management

Conduct pre-study, site qualification, study initiation, monitoring, and close-out activities

Maintain accurate source documentation and report adverse events in accordance with regulatory requirements

Recruit, screen, enroll, and obtain informed consent from study participants

Collect, manage, and maintain patient and laboratory data

Work directly with study participants and their families and serve as a liaison to internal departments, external organizations, and government agencies

Perform all duties under the direction of the Lead Study Coordinator and Primary Investigators (PI)